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Haemodynamic optimisation of a dialysis graft design using a global optimisation approach

Disturbed flow and the resulting non‐physiological wall shear stress (WSS) at the graft‐vein anastomosis play an important role in arteriovenous graft (AVG) patency loss. Modifying graft geometry with helical features is a popular approach to minimise the occurrence of detrimental haemodynamics and...

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Autores principales: Quicken, Sjeng, Delhaas, Tammo, Mees, Barend M. E., Huberts, Wouter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900962/
https://www.ncbi.nlm.nih.gov/pubmed/33249781
http://dx.doi.org/10.1002/cnm.3423
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author Quicken, Sjeng
Delhaas, Tammo
Mees, Barend M. E.
Huberts, Wouter
author_facet Quicken, Sjeng
Delhaas, Tammo
Mees, Barend M. E.
Huberts, Wouter
author_sort Quicken, Sjeng
collection PubMed
description Disturbed flow and the resulting non‐physiological wall shear stress (WSS) at the graft‐vein anastomosis play an important role in arteriovenous graft (AVG) patency loss. Modifying graft geometry with helical features is a popular approach to minimise the occurrence of detrimental haemodynamics and to potentially increase graft longevity. Haemodynamic optimisation of AVGs typically requires many computationally expensive computational fluid dynamics (CFD) simulations to evaluate haemodynamic performance of different graft designs. In this study, we aimed to develop a haemodynamically optimised AVG by using an efficient meta‐modelling approach. A training dataset containing CFD evaluations of 103 graft designs with helical features was used to develop computationally low‐cost meta‐models for haemodynamic metrics related to graft dysfunction. During optimisation, the meta‐models replaced CFD simulations that were otherwise needed to evaluate the haemodynamic performance of possible graft designs. After optimisation, haemodynamic performance of the optimised graft design was verified using a CFD simulation. The obtained optimised graft design contained both a helical graft centreline and helical ridge. Using the optimised design, the magnitude of flow disturbances and the size of the anastomotic areas exposed to non‐physiological WSS was successfully reduced compared to a regular straight graft. Our meta‐modelling approach allowed to reduce the total number of CFD model evaluations required for our design optimisation by approximately a factor 2000. The applied efficient meta‐modelling technique was successful in identifying an optimal, helical graft design at relatively low computational costs. Future studies should evaluate the in vivo benefits of the developed graft design.
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spelling pubmed-79009622021-03-03 Haemodynamic optimisation of a dialysis graft design using a global optimisation approach Quicken, Sjeng Delhaas, Tammo Mees, Barend M. E. Huberts, Wouter Int J Numer Method Biomed Eng Research Article ‐ Applications Disturbed flow and the resulting non‐physiological wall shear stress (WSS) at the graft‐vein anastomosis play an important role in arteriovenous graft (AVG) patency loss. Modifying graft geometry with helical features is a popular approach to minimise the occurrence of detrimental haemodynamics and to potentially increase graft longevity. Haemodynamic optimisation of AVGs typically requires many computationally expensive computational fluid dynamics (CFD) simulations to evaluate haemodynamic performance of different graft designs. In this study, we aimed to develop a haemodynamically optimised AVG by using an efficient meta‐modelling approach. A training dataset containing CFD evaluations of 103 graft designs with helical features was used to develop computationally low‐cost meta‐models for haemodynamic metrics related to graft dysfunction. During optimisation, the meta‐models replaced CFD simulations that were otherwise needed to evaluate the haemodynamic performance of possible graft designs. After optimisation, haemodynamic performance of the optimised graft design was verified using a CFD simulation. The obtained optimised graft design contained both a helical graft centreline and helical ridge. Using the optimised design, the magnitude of flow disturbances and the size of the anastomotic areas exposed to non‐physiological WSS was successfully reduced compared to a regular straight graft. Our meta‐modelling approach allowed to reduce the total number of CFD model evaluations required for our design optimisation by approximately a factor 2000. The applied efficient meta‐modelling technique was successful in identifying an optimal, helical graft design at relatively low computational costs. Future studies should evaluate the in vivo benefits of the developed graft design. John Wiley & Sons, Inc. 2020-12-09 2021-02 /pmc/articles/PMC7900962/ /pubmed/33249781 http://dx.doi.org/10.1002/cnm.3423 Text en © 2020 The Authors. International Journal for Numerical Methods in Biomedical Engineering published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Article ‐ Applications
Quicken, Sjeng
Delhaas, Tammo
Mees, Barend M. E.
Huberts, Wouter
Haemodynamic optimisation of a dialysis graft design using a global optimisation approach
title Haemodynamic optimisation of a dialysis graft design using a global optimisation approach
title_full Haemodynamic optimisation of a dialysis graft design using a global optimisation approach
title_fullStr Haemodynamic optimisation of a dialysis graft design using a global optimisation approach
title_full_unstemmed Haemodynamic optimisation of a dialysis graft design using a global optimisation approach
title_short Haemodynamic optimisation of a dialysis graft design using a global optimisation approach
title_sort haemodynamic optimisation of a dialysis graft design using a global optimisation approach
topic Research Article ‐ Applications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900962/
https://www.ncbi.nlm.nih.gov/pubmed/33249781
http://dx.doi.org/10.1002/cnm.3423
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